Cells throughout our body are exposed to various forms of mechanical stimuli[1, 2]. To examine effects of mechanical cyclic strain on vascular cells, several types of strain devices have been developed, and the methods of force application range from use of dynamic indenters[3] to vacuum pressures (both positive[4] or negative[5, 6]) to stretch the bottom surface of the elastic substrate to which the cells are cultured. A number of custom uniaxial strain devices have been developed to examine cells that are normally exposed to lateral stresses[7–11]. However, a limitation to most uniaxial strain devices is that they can only accommodate a limited number of samples[8–12] at one time. Most devices also lack a platform to perform consistent clamping and loading of samples, which can significantly alter substrate strain[8, 9, 13] and ultimately, introduce large variations between experiments. Here we present a computer controlled precision strain application system composed of a custom multi-well uniaxial Cellular Strain Assessment Tool (CSAT) (Figure 1), a microscope adaptable mini CSAT, and custom elastomeric polydimethylsiloxane (PDMS) plates. The effect of cyclic tensile strain on the migration of endothelial cells was also analyzed in this study. Human umbilical vein endothelial cells (HUVECs), cultured in 2D directly on elastomeric polydimethylsiloxane (PDMS) substrates were exposed to cyclic tensile strain at physiologic levels, and demonstrated to enhance EC migration.
Tumor necrosis factor ?-dependent proinflammatory gene induction is inhibited by cyclic tensile strain in articular chondrocytes in vitro
